Q92.62

The ICD-10-CM code for marker chromosomes in abnormal individual is Q92.62. The full clinical description is "Marker chromosomes in abnormal individual". Q92.62 is a billable/specific code that can be used on insurance claims and medical billing.

ICD-10-CM code Q92.62 represents “Marker chromosomes in abnormal individual”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Yes, Q92.62 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

Q92.62 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

Q92.62 has Excludes1 notes indicating codes that cannot be used together with it, including: trisomies of chromosomes 13, 18, 21 (Q90-Q91).

Q92.62 is linked to 1 UMLS Concept Unique Identifier: C2910364. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like marker chromosomes in abnormal individual affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

There is no direct ICD-11 mapping available for Q92.62 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.